JP2002347180A - Coextrusion film or the like, and tape products and manufactured goods or the like including them - Google Patents
Coextrusion film or the like, and tape products and manufactured goods or the like including themInfo
- Publication number
- JP2002347180A JP2002347180A JP2002066392A JP2002066392A JP2002347180A JP 2002347180 A JP2002347180 A JP 2002347180A JP 2002066392 A JP2002066392 A JP 2002066392A JP 2002066392 A JP2002066392 A JP 2002066392A JP 2002347180 A JP2002347180 A JP 2002347180A
- Authority
- JP
- Japan
- Prior art keywords
- adhesive
- film
- layer
- tape product
- base layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000853 adhesive Substances 0.000 claims abstract description 29
- 239000000463 material Substances 0.000 claims abstract description 11
- 238000000576 coating method Methods 0.000 claims abstract description 7
- 239000011248 coating agent Substances 0.000 claims abstract description 6
- 230000001070 adhesive effect Effects 0.000 claims description 27
- 230000003014 reinforcing effect Effects 0.000 claims description 27
- -1 polyethylene Polymers 0.000 claims description 23
- 239000004698 Polyethylene Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 229920000573 polyethylene Polymers 0.000 claims description 10
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 9
- 239000005871 repellent Substances 0.000 claims description 5
- 244000043261 Hevea brasiliensis Species 0.000 claims description 3
- 239000004831 Hot glue Substances 0.000 claims description 3
- 239000003522 acrylic cement Substances 0.000 claims description 3
- 229920003052 natural elastomer Polymers 0.000 claims description 3
- 229920001194 natural rubber Polymers 0.000 claims description 3
- 238000004806 packaging method and process Methods 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 229920003051 synthetic elastomer Polymers 0.000 claims description 3
- 239000005061 synthetic rubber Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 2
- 239000002390 adhesive tape Substances 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 76
- 229920001577 copolymer Polymers 0.000 description 19
- 239000004743 Polypropylene Substances 0.000 description 13
- 229920001155 polypropylene Polymers 0.000 description 13
- 229920000092 linear low density polyethylene Polymers 0.000 description 11
- 239000004707 linear low-density polyethylene Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 9
- 239000005038 ethylene vinyl acetate Substances 0.000 description 7
- 230000002787 reinforcement Effects 0.000 description 7
- 239000012758 reinforcing additive Substances 0.000 description 7
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 6
- 229920002725 thermoplastic elastomer Polymers 0.000 description 6
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000000654 additive Substances 0.000 description 4
- 239000012790 adhesive layer Substances 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000011247 coating layer Substances 0.000 description 3
- 229920001384 propylene homopolymer Polymers 0.000 description 3
- 239000012744 reinforcing agent Substances 0.000 description 3
- 230000002940 repellent Effects 0.000 description 3
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 229920005653 propylene-ethylene copolymer Polymers 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 241001272567 Hominoidea Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 206010061592 cardiac fibrillation Diseases 0.000 description 1
- 235000019504 cigarettes Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000001862 defibrillatory effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000005026 oriented polypropylene Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000012745 toughening agent Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/12—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by using adhesives
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B37/00—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding
- B32B37/14—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers
- B32B37/15—Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with at least one layer being manufactured and immediately laminated before reaching its stable state, e.g. in which a layer is extruded and laminated while in semi-molten state
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/20—Adhesives in the form of films or foils characterised by their carriers
- C09J7/22—Plastics; Metallised plastics
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J7/00—Adhesives in the form of films or foils
- C09J7/30—Adhesives in the form of films or foils characterised by the adhesive composition
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/24—All layers being polymeric
- B32B2250/242—All polymers belonging to those covered by group B32B27/32
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/10—Coating on the layer surface on synthetic resin layer or on natural or synthetic rubber layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2270/00—Resin or rubber layer containing a blend of at least two different polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2323/00—Polyalkenes
- B32B2323/04—Polyethylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2323/00—Polyalkenes
- B32B2323/10—Polypropylene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2405/00—Adhesive articles, e.g. adhesive tapes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J2301/00—Additional features of adhesives in the form of films or foils
- C09J2301/10—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet
- C09J2301/12—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers
- C09J2301/122—Additional features of adhesives in the form of films or foils characterized by the structural features of the adhesive tape or sheet by the arrangement of layers the adhesive layer being present only on one side of the carrier, e.g. single-sided adhesive tape
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Adhesive Tapes (AREA)
- Wrappers (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
Description
【0001】発明の背景 1.発明の分野 本発明は、共押出(同時押出、co-extruded)フィルム
の製造方法、それによって製造されたフィルム、該フィ
ルムを包含するテープ製品類、および、該テープ製品類
の用途に関する。BACKGROUND OF THE INVENTION FIELD OF THE INVENTION The present invention relates to a method for producing a co-extruded film, a film produced thereby, tape products including the film, and uses of the tape products.
【0002】2.関連技術の説明 一軸延伸ポリプロピレン(”MOPP”)フィルム類は
周知である。これらのフィルム類は、代表的には、ポリ
プロピレン粒(granules)をフィルムダイに通して加工
することによって粗大(bulky)前駆体フィルムを作
り、次いで該前駆体フィルムを、例えば、ロール型延伸
フレーム(roll-type drawing frame)上で、一方向に
延伸することによって最終的なMOPPフィルム類を造
り出す工程によって製造される。[0002] 2. 2. Description of the Related Art Uniaxially oriented polypropylene ("MOPP") films are well known. These films are typically made into bulk precursor films by processing polypropylene granules through a film die and then forming the precursor films into, for example, a roll-type stretch frame ( On a roll-type drawing frame), it is manufactured by a process of producing a final MOPP film by stretching in one direction.
【0003】延伸操作はMOPPフィルム類を”配行”
させ、その結果、それらは一般に延伸の方向の引張強度
が大きいこと特徴とする。同時に、これらのMOPPフ
ィルム類は、延伸方向に垂直の横方向に許容できない弱
さがあることを特徴とする。[0003] The stretching operation is "arranging" MOPP films.
As a result, they are generally characterized by a high tensile strength in the direction of stretching. At the same time, these MOPP films are characterized by an unacceptable weakness in the transverse direction perpendicular to the stretching direction.
【0004】該フィルム類をテープ類やその他の製品類
へと裁断すると、どちらかの長手方向のエッジに沿っ
て”微細切り目(micronicks)”が現れることがある。
フィルムが横方向に弱いために、これらの微細切り目は
横方向に拡大し、究極的には破断に至る傾向にある。[0004] When the films are cut into tapes or other products, "micronicks" may appear along either longitudinal edge.
Because the film is weak in the transverse direction, these micro-cuts tend to expand in the transverse direction, ultimately leading to breakage.
【0005】その全開示をここに参照文献として援用す
るエンゲルマン等(Engelmann et al.)の米国特許第
5,093,187号では、例えば、ポリエチレンフィ
ルムの層と共にポリプロピレンフィルムを共押出してこ
の問題を解決している。この第二層は微細切り目の形成
に対して抵抗性がある点で、該第二層の方がポリプロピ
レンフィルム”よりも強靭”である。該第二層がポリプ
ロピレン層に接着されているため、ポリプロピレン層に
微細切り目が生じないか、微細切り目が生じても横方向
に進展することがなく、その結果、いずれの場合もこの
様な共押出テープ類はより破断し難くなる。In US Pat. No. 5,093,187 to Engelmann et al., The entire disclosure of which is incorporated herein by reference, for example, co-extruding a polypropylene film with a layer of polyethylene film co-extrudes this problem. Has been resolved. This second layer is more tough than the polypropylene film in that it is resistant to the formation of fine cuts. Since the second layer is adhered to the polypropylene layer, no fine cuts are formed in the polypropylene layer, or even if the fine cuts are formed, they do not develop in the lateral direction. Extruded tapes are more difficult to break.
【0006】エンゲルマン等は、最も好ましい構造が、
共押出フィルムの厚みの65〜75%をポリプロピレン
基層(base layer or layers)が占めるようにしたもの
であることを教えており、このことは第二層、例えば、
同時押出されたポリエチレン層が残余の25〜35%を
占めるべきことを意味する。第5欄第16〜21行を参
照のこと。従って、例えば、最も好ましいフィルム類は
実施例のものであるが、これらは合計厚み83〜87μ
mで、そのうち60〜63μmの厚みがポリプロピレン
基層であることを特徴とし、このことは残余の20〜2
7μmの厚みが第二層であることを意味する。特に第6
欄第29〜33行を参照のこと。[0006] Engelman et al.
Teaches that the base layer or layers occupy 65 to 75% of the thickness of the coextruded film, which indicates that the second layer, e.g.
It means that the coextruded polyethylene layer should make up the remaining 25-35%. See column 5, lines 16-21. Thus, for example, the most preferred films are those of the examples, but these have a total thickness of 83-87 μm.
m, of which the thickness of 60 to 63 μm is the polypropylene base layer, which is the remaining 20 to 2 μm.
A thickness of 7 μm means the second layer. Especially the sixth
See column lines 29-33.
【0007】本出願人は、これらの比率で作製されたフ
ィルム類が縦方向の破断点伸びが許容できない程大きい
ことを特徴とし、このことが幾つかの目的に対して該フ
ィルム類を不適なものにしていることを発見した。例え
ば、これらのテープ類を封筒類や箱類等の閉鎖構造物類
を引き裂き開けるのに用いる。これらのテープ類は製造
ライン上で閉鎖構造物類に貼付けられる。望ましい高い
ライン速度(line speeds)では、これらのフィルム類
は長手方向に沿って引っ張られ、閉鎖構造物の一部分の
上で延伸され、それから該構造物に接着されて裁断され
る。縦方向の破断点伸びが許容できない程大きいので、
これらテープ類はゴムバンドの様な性質を示し、裁断時
にはね返り、閉鎖構造物への被覆(coverage)が不適切
なものとなる。Applicants have characterized that films made at these ratios have unacceptably high elongation at break in the longitudinal direction, which makes them unsuitable for some purposes. I discovered what I was doing. For example, these tapes are used to tear open closed structures such as envelopes and boxes. These tapes are applied to closed structures on the production line. At the desired high line speeds, these films are pulled longitudinally, stretched over a portion of a closed structure, and then glued to the structure and cut. Since the elongation at break in the longitudinal direction is unacceptably large,
These tapes exhibit rubber band-like properties, rebound when cut, and provide inadequate coverage for closed structures.
【0008】実際は、縦方向の破断点伸びは35%を越
えるべきではなく、ところがそれは、エンゲルマン等が
示したものは非共押出比較テープ類A、B及びCによっ
て示されていることである。第8欄第41行以降の表1
を参照のこと。対照として、エンゲルマン等のテープ類
は、縦方向の破断点伸びが少なくとも40%であること
を特徴とすると報告されているが、この特許範囲内の商
業的実施態様は縦方向の破断点伸びが少なくとも55%
であることを特徴としているのを本出願人は発見した。In practice, the elongation at break in the longitudinal direction should not exceed 35%, which is what Engelman et al. Showed by non-coextruded comparative tapes A, B and C. . Table 1 from column 8, line 41
checking ... As a control, tapes such as Engelman et al. Are reported to be characterized by an elongation at break in the longitudinal direction of at least 40%, although commercial embodiments within the patent range include elongation at break in the longitudinal direction. Is at least 55%
Applicants have discovered that
【0009】MOPPフィルム類、特にそれらから製造
された接着テープ類に関連するもう一つの問題は、ロー
ルから巻き出される際にかかるテープ類は”破砕(shre
dding)”や”フィブリル化(fibrillation)”の特徴
があることである。ロール状に巻き取る際は、接着剤層
がポリプロピレン層に接着されることになり、そのため
にテープをロールから巻き出す際には接着剤がポリプロ
ピレン層のフィラメントを引き剥がし、その結果テープ
が破砕された外観となる。テープの審美的外観が大きく
損なわれるのみならず、接着剤にくっ付いたこれらの破
片の存在のために、かかる破片が多数ある場合には粘着
性(tack)の大きな減少を招くことになる。Another problem associated with MOPP films, especially adhesive tapes made therefrom, is that when unwound from a roll, such tapes are "shreated."
It has the characteristics of “dding” or “fibrillation.” When wound up in a roll, the adhesive layer is bonded to the polypropylene layer, which causes the tape to be unwound from the roll. The adhesive peels off the filaments of the polypropylene layer, resulting in a shattered appearance of the tape, which not only greatly impairs the aesthetic appearance of the tape, but also due to the presence of these debris sticking to the adhesive In addition, a large number of such fragments will lead to a large decrease in tack.
【0010】エンゲルマン等は、この問題を、接着剤が
コーティングされていないフィルムの片面上に接着剤反
発性(adhesive-repellant)の剥離層をコーティングす
ることによって解決した。第5欄第66〜68行を参照
のこと。しかし、実施例では、市販のシリコーン剥離ラ
ッカーを使用している。第6欄第39〜42行を参照の
こと。シリコーン剥離ラッカー類を用いると、生産コス
トと乾燥時間を増大させ、製造速度を低下させる。[0010] Engelmann et al. Solved this problem by coating an adhesive-repellant release layer on one side of the uncoated adhesive film. See col. 5, lines 66-68. However, the examples use a commercially available silicone release lacquer. See column 6, lines 39-42. The use of silicone release lacquers increases production costs and drying times and reduces production rates.
【0011】発明の要約 従って、本発明の一つの目的は、市場の従来の非共押出
フィルム類によって発現されるのと同様の縦方向の破断
点伸び性、即ち約35%を越えない縦方向の破断点伸び
を有する共押出フィルムを提供することである。SUMMARY OF THE INVENTION Accordingly, one object of the present invention is to provide a longitudinal elongation at break similar to that exhibited by conventional non-coextruded films on the market, ie, not exceeding about 35%. The purpose of the present invention is to provide a coextruded film having an elongation at break.
【0012】本発明のもう一つの目的は、接着剤反発性
剥離層を全く必要としないか、さもなくばより安価でよ
り効率的に適用できる接着剤反発性剥離コーティング類
を組み込んだ共押出接着テープを提供することである。Another object of the present invention is to provide coextrusion adhesives that do not require any adhesive repellent release layer or incorporate adhesive repellent release coatings that would otherwise be cheaper and more efficient to apply. Is to provide tape.
【0013】これらや他の目的は本発明により達成さ
れ、その第一の実施態様は、(A)基層、および、
(B)(A)に接着された補強層を包含するフィルムで
あって、(B)は(A)よりも強靭な材料から成り、
(B)は(A)の表面上に連続層を形成し、且つ、
(B)の厚みは(A)+(B)の合計厚みの25%より
小さいフィルムに関する。[0013] These and other objects are achieved by the present invention, a first embodiment of which comprises (A) a base layer, and
(B) a film including a reinforcing layer adhered to (A), wherein (B) is made of a tougher material than (A);
(B) forms a continuous layer on the surface of (A), and
The thickness of (B) relates to a film that is less than 25% of the total thickness of (A) + (B).
【0014】ここで、補強層(B)が、基層(A)”よ
りも強靭な”材料から成ると記述されているのは、基層
(A)の脆性破壊を既に招いている衝撃荷重を受けた時
に補強層(B)が破壊無しに変形することを意味してい
る。従って、補強層(B)は、より高い衝撃強度、伸び
及びエネルギー吸収性を有するのが好ましい。The reason why the reinforcing layer (B) is described as being made of a material which is more tough than the "base layer (A)" is that the reinforcing layer (B) is subjected to an impact load which has already caused brittle fracture of the base layer (A). Means that the reinforcing layer (B) is deformed without breaking. Accordingly, the reinforcing layer (B) preferably has higher impact strength, elongation and energy absorption.
【0015】エンゲルマン等によって開示されたフィル
ム類と比べて、本発明フィルム類は、顕著なフィルム特
性によって特徴づけられる。上述のことから分かる様
に、エンゲルマン等により開示されたフィルム類は少な
くとも40%の縦方向の破断点伸びにより特徴づけられ
ると報告され、また、この特許の範囲に入る商業的実施
態様は少なくとも55%の縦方向の破断点伸びによって
特徴づけられるのに対し、本発明フィルム類は約35%
を越えない縦方向の破断点伸びであることを特徴とす
る。Compared to the films disclosed by Engelman et al., The films of the present invention are characterized by outstanding film properties. As can be seen from the foregoing, the films disclosed by Engelman et al. Are reported to be characterized by an elongation at break in the machine direction of at least 40%, and commercial embodiments falling within the scope of this patent are at least The films of the present invention are characterized by about 35% elongation at break in the longitudinal direction of 55%.
The elongation at break in the longitudinal direction that does not exceed.
【0016】驚くべきことに、本発明フィルム類の改善
された特性は、引張強度の損失無しに達成される。従っ
て、例えば、本発明に従って製作した63μm厚みのフ
ィルム類は、縦方向に測定して、70〜80N/4mm
の極限引張応力を示した。これに対して、厚みを83〜
85μmに変えたエンゲルマン等の例示されたフィルム
類は、65〜73N/4mmの極限引張応力を示した。
引張強度は厚みが増加するにつれてほぼ直線的に増大す
るので、本発明フィルム類のより高い引張応力は驚くべ
きことである。従って、本発明フィルムを薄くしていけ
ばより低い引張強度を示すことが予測されるが、これは
観察されなかった。Surprisingly, the improved properties of the films of the present invention are achieved without loss of tensile strength. Thus, for example, 63 μm thick films made in accordance with the present invention have a thickness of 70-80 N / 4 mm, measured in the longitudinal direction.
The ultimate tensile stress of On the other hand, the thickness is 83 ~
Exemplified films, such as Engelman, changed to 85 μm showed ultimate tensile stress of 65-73 N / 4 mm.
The higher tensile stress of the films of the present invention is surprising since the tensile strength increases almost linearly with increasing thickness. Therefore, it is expected that the thinner the inventive film, the lower the tensile strength, but this was not observed.
【0017】発明の詳細な説明 一般的には、基層と補強層の材料類の選定はエンゲルマ
ン等に記載されている通りである。本発明フィルム類と
エンゲルマンのフィルム類の主たる差異は、補強層の厚
みとそれに由来する特性にある。本発明フィルム類は、
多層の基層及び補強層からなっていてもよいが、この場
合、全ての基層及び補強層の合計厚みは、ここに記載さ
れるパラメーターを越えるべきではない。DETAILED DESCRIPTION OF THE INVENTION Generally, the selection of materials for the base layer and the reinforcing layer is as described in Engelmann et al. The main difference between the films of the present invention and Engelman's films lies in the thickness of the reinforcing layer and the properties derived therefrom. The films of the present invention are:
It may consist of multiple base layers and reinforcement layers, in which case the total thickness of all base layers and reinforcement layers should not exceed the parameters described here.
【0018】従って、基層はポリプロピレン−オレフィ
ン共重合体及び/又はポリプロピレン−強化用添加剤
(toughening additive)混合物から構成される。好ま
しい実施態様においては、基層は、耐衝撃性変性ポリプ
ロピレンを主に、好ましくは少なくとも70%含む。こ
の目的のために、プロピレン及びオレフィン類のランダ
ム又はブロック共重合体類を用いるのが好ましい。Accordingly, the base layer is composed of a polypropylene-olefin copolymer and / or a polypropylene-toughening additive mixture. In a preferred embodiment, the base layer comprises mainly impact-modified polypropylene, preferably at least 70%. For this purpose, preference is given to using random or block copolymers of propylene and olefins.
【0019】基層は100%までのプロピレン−オレフ
ィン共重合体類を含んでもよく、また、これらの共重合
体類と混合して25%までの強化用添加剤を含んでもよ
い。これは、ポリプロピレンの横方向の衝撃引張強度を
向上させるのに適している。好ましい強化用添加剤類
は、リニア(linear)低密度ポリエチレン(LLDP
E)、ブタジエン−スチレン共重合体類(SBS)やイ
ソプレン−スチレン共重合体類(SIS)、特に各場合
においてそれらのブロック共重合体類などの熱可塑性ゴ
ム類、または、エチレン−酢酸ビニル(EVA)であ
る。The base layer may contain up to 100% of propylene-olefin copolymers and may contain up to 25% of reinforcing additives in admixture with these copolymers. This is suitable for improving the transverse impact tensile strength of polypropylene. Preferred toughening additives are linear low density polyethylene (LLDP)
E), thermoplastic rubbers such as butadiene-styrene copolymers (SBS) and isoprene-styrene copolymers (SIS), in particular, in each case, block copolymers thereof, or ethylene-vinyl acetate ( EVA).
【0020】基層はポリプロピレン単独重合体を含んで
もよいが、その際は強化用添加剤も好ましくは少なくと
も10%であるが30%を越えない様に含む。The base layer may comprise a polypropylene homopolymer, in which case the reinforcing additives are also preferably present in at least 10% but not more than 30%.
【0021】プロピレン−オレフィン共重合体類とプロ
ピレン単独重合体の混合物類を用いることもできる。こ
の実施態様では、強化用添加剤類の比率は共重合体の比
率の上昇に従って減少させてもよい。Mixtures of propylene-olefin copolymers and propylene homopolymer can also be used. In this embodiment, the proportion of reinforcing additives may be reduced as the proportion of copolymer increases.
【0022】強化剤類(toughening agents)は個々に
添加するのが好ましい。しかし、強化剤類の混合物類を
用いることもできる。Preferably, the toughening agents are added individually. However, mixtures of reinforcing agents can also be used.
【0023】基層は、共重合体を75〜100%及びL
LDPEを25〜0%、または、共重合体を80〜10
0%及び熱可塑性ゴム、特にSBS又はSISを20〜
0%、または、共重合体を75〜100%及びEVAを
25〜0%含むのが好ましい。特に好ましいのは、80
〜95%の共重合体及び5〜20%のLLDPE、また
は、85〜95%の共重合体及び5〜15%の熱可塑性
ゴム、特にSBS又はSIS、または、85〜95%の
共重合体及び5〜15%のEVAのブレンドである。The base layer contains 75 to 100% of a copolymer and L
LDPE is 25 to 0%, or copolymer is 80 to 10%.
0% and a thermoplastic rubber, especially SBS or SIS of 20 to
Preferably, it contains 0% or 75 to 100% of a copolymer and 25 to 0% of EVA. Particularly preferred is 80
-95% copolymer and 5-20% LLDPE, or 85-95% copolymer and 5-15% thermoplastic rubber, especially SBS or SIS, or 85-95% copolymer And a blend of 5-15% EVA.
【0024】特に好ましい実施態様においては、基層は
プロピレン−エチレン共重合体を含み、これを強化剤と
してのリニア低密度ポリエチレンとブレンドし、共重合
体対ブレンドされたポリエチレンの比を75:25〜9
5:5、好ましくは90:10〜95:5の範囲とす
る。In a particularly preferred embodiment, the base layer comprises a propylene-ethylene copolymer, which is blended with a linear low density polyethylene as a reinforcing agent to provide a copolymer to blended polyethylene ratio of from 75:25 to 75:25. 9
5: 5, preferably in the range of 90:10 to 95: 5.
【0025】基層上に配置される強化層用としては、好
ましくは、強化用添加剤を明らかにより高い比率で含む
か、基層よりも高い衝撃引張強度によって特徴づけられ
るか、あるいは両方かの材料類の混合物類が用いられ
る。強化層は、基層用として明記した様な、ポリプロピ
レンを、特に65%までのプロピレン−オレフィン共重
合体又は55%までのプロピレン単独重合体を含み、各
場合において好ましくは少なくとも20%含むのが好ま
しく、これに好ましくは35又は45〜80%の強化用
添加剤、特にLLDPE、熱可塑性ゴム類又はEVAを
添加する。強化用添加剤類は個々に添加するのが好まし
い。しかし、再び、強化用添加剤類の混合物類も用いる
ことができる。ここでもまた、ポリプロピレン−オレフ
ィン共重合体類とプロピレン単独重合体の混合物類も用
いることができる。基層におけると同様に、強化用添加
剤は、衝撃引張強度の特にその横方向における向上をも
たらす。For the reinforcing layer disposed on the base layer, it is preferred that it comprises a distinctly higher proportion of reinforcing additives, is characterized by a higher impact tensile strength than the base layer, or both materials. Are used. The reinforcing layer comprises polypropylene, as specified for the base layer, in particular up to 65% of propylene-olefin copolymer or up to 55% of propylene homopolymer, preferably in each case preferably at least 20% , To which 35 or 45 to 80% of reinforcing additives, in particular LLDPE, thermoplastic rubbers or EVA are added. Preferably, the reinforcing additives are added individually. However, again, mixtures of reinforcing additives can be used. Again, mixtures of polypropylene-olefin copolymers and propylene homopolymers can be used. As in the base layer, the toughening additive provides an improvement in impact tensile strength, especially in its transverse direction.
【0026】強化層は、共重合体を20〜50%及びL
LDPEを80〜50%、または、共重合体を50〜7
0%及び熱可塑性ゴム、特にSBS又はSISを50〜
30%、または、共重合体を20〜40%及びEVAを
80〜60%含むのが好ましいが、強化層が、共重合体
を30〜40%及びLLDPEを60〜70%、また
は、共重合体を55〜65%及び熱可塑性ゴム、特にS
BS又はSISを35〜45%、または、共重合体を2
5〜35%及びEVAを65〜75%含むのが特に好ま
しい。The reinforcing layer contains 20 to 50% of the copolymer and L
LDPE 80 to 50%, or copolymer 50 to 7
0% and thermoplastic rubber, especially SBS or SIS 50 to 50%
Preferably, it contains 30% or 20-40% copolymer and 80-60% EVA, but the reinforcing layer is 30-40% copolymer and 60-70% LLDPE or copolymer. 55-65% coalescing and thermoplastic rubber, especially S
35 to 45% of BS or SIS, or 2% of copolymer
It is particularly preferred to contain 5 to 35% and 65 to 75% EVA.
【0027】特に好ましい実施態様においては、強化層
はプロピレン−エチレン共重合体を含むが、これをリニ
ア低密度ポリエチレンとブレンドし、共重合体対ブレン
ドされたポリエチレンの比を50:50〜25:75、
好ましくは40:60〜30:70の範囲とする。In a particularly preferred embodiment, the reinforcing layer comprises a propylene-ethylene copolymer, which is blended with a linear low density polyethylene to provide a copolymer to blended polyethylene ratio of from 50:50 to 25:25. 75,
Preferably, it is in the range of 40:60 to 30:70.
【0028】層間の良好な適合性(compatibility)の
ためには、基層及び強化層に同一の強化剤(toughening
agent)を用いるのが好ましい。しかし、それぞれ異な
った強化剤類を用いたり、強化剤類の異なった混合物類
を用いることも可能である。For good compatibility between the layers, the same toughening is used for the base layer and the reinforcing layer.
agent). However, it is also possible to use different fortifiers or to use different mixtures of fortifiers.
【0029】特にそれを意図されているLLDPEは、
少なくとも3個、好ましくは3〜10個の炭素原子を含
むオレフィンを用いて共重合した、密度約0.910〜
0.935g/cm3の特殊のエチレン共重合体であ
る。エル・シュヴィ−ク(L.Schwiegk):”LLDP
E−ein neues Polyathylen(LLDPE-新しいポリエ
チレン)”、Plastverarbeiter(プラスチック類の二次
加工業者)、第33年度(33rd year)、1982、N
o.9、1035〜1037頁を参照のこと。LLDPE specifically intended for it is
Having a density of about 0.910, copolymerized with an olefin containing at least 3, preferably 3 to 10 carbon atoms.
It is a special ethylene copolymer of 0.935 g / cm 3 . L. Schwiegk: "LLDP
E-ein neues Polyathylen (LLDPE-new polyethylene) ", Plastverarbeiter (secondary processor of plastics), 33rd year, 1982, N
o. See pages 9,1035-1037.
【0030】本発明による好ましい基材フィルム類用と
しては、コモノマーとして1−オクテンを有するLLD
PEであって、0.920g/cm3前後の密度を有す
るものを用いる。For preferred substrate films according to the present invention, LLDs having 1-octene as comonomer
PE having a density of about 0.920 g / cm 3 is used.
【0031】50%前後のスチレン含量を有するブロッ
ク共重合体をブタジエンースチレン強化剤として用いる
のが好ましい。同様に作用するスチレン−イソプレン共
重合体類を用いるのも同様に可能である。It is preferred to use a block copolymer having a styrene content of around 50% as a butadiene-styrene reinforcing agent. It is likewise possible to use styrene-isoprene copolymers which act in a similar manner.
【0032】EVA共重合体として約45%のビニール
含量を有するポリマーを用いるのが好ましい。Preferably, a polymer having a vinyl content of about 45% is used as the EVA copolymer.
【0033】基層類及び/又は強化層類は、更なる適当
なポリマー類及び/又は通常の添加剤類をより小さな比
率、好ましくは10%まで、特には5%まで更に含んで
もよい。The base layers and / or reinforcing layers may furthermore contain further suitable polymers and / or customary additives in a smaller proportion, preferably up to 10%, in particular up to 5%.
【0034】本発明フィルム類は、個々の層からなる材
料類を共押出一次フィルムに同時押し出し、次いで通常
の技術を用いて少なくとも一方向に該一次フィルムを延
伸することによって得るのが好ましい。個々の層を押し
出して延伸し、次いで該個々の層を互いにラミネートす
ることも可能である。延伸は縦方向に行うのが好まし
い。The films of the present invention are preferably obtained by co-extruding the material of the individual layers into a coextruded primary film, and then stretching the primary film in at least one direction using conventional techniques. It is also possible to extrude and stretch the individual layers and then laminate the individual layers together. Stretching is preferably performed in the machine direction.
【0035】エンゲルマンの第5欄第3〜13行によっ
て定義される縦方向の延伸比は、1:5〜1:9である
のが好ましく、特には1:6.5〜1:7.5である。The stretch ratio in the machine direction, as defined by column 5, lines 3 to 13 of Engelmann, is preferably from 1: 5 to 1: 9, in particular from 1: 6.5 to 1: 7. 5
【0036】最終的なフィルムの厚みは、全補強層の合
計厚みがフィルム全体の厚みの25%よりも小さく、好
ましくは15%よりも小さく、特に好ましくは10%よ
りも小さい様なものである。次に図1を参照すると、基
層11と補強層12からなる本発明によるフィルム10
の断面が示されている。好ましい実施態様においては、
基層11の厚みは約60μm〜約125μmの範囲にあ
り、補強層12の厚みは約2μm〜約10μmの範囲に
ある。複数の基層及び/又は複数の補強層がある場合に
は、基層の合計厚みは約60μm〜約125μmの範囲
にあり、補強層の合計厚みは約2μm〜約10μmの範
囲にある。特に好ましい実施態様においては、厚み約6
0μm〜約125μmの範囲にある単一の基層及び厚み
約3μm〜約5μmの範囲にある単一の補強層がある。The final film thickness is such that the total thickness of all the reinforcing layers is less than 25%, preferably less than 15%, particularly preferably less than 10% of the total film thickness. . Referring now to FIG. 1, a film 10 according to the present invention comprising a base layer 11 and a reinforcing layer 12 is shown.
Is shown. In a preferred embodiment,
The thickness of the base layer 11 is in a range from about 60 μm to about 125 μm, and the thickness of the reinforcing layer 12 is in a range from about 2 μm to about 10 μm. If there is more than one base layer and / or more than one reinforcement layer, the total thickness of the base layers is in the range of about 60 μm to about 125 μm, and the total thickness of the reinforcement layers is in the range of about 2 μm to about 10 μm. In a particularly preferred embodiment, a thickness of about 6
There is a single base layer ranging from 0 μm to about 125 μm and a single reinforcing layer ranging from about 3 μm to about 5 μm in thickness.
【0037】次に図2を参照すると、本発明フィルム類
をテープ製品20中に組み込むことができ、該テープ製
品は前述の有利な特性を示す。この図に描かれたテープ
製品は、基層11、補強層12、接着剤層21、プライ
マー層22、および、任意に設ける接着剤反発性剥離コ
ーティング層23からなる。接着剤層、プライマー層、
および、任意に設ける剥離コーティング層用としては、
如何なる通常の材料類を用いてもよい。この接着剤は、
天然ゴム系接着剤、合成ゴム系接着剤及びアクリル系接
着剤からなる群から選ぶのが好ましく、また、ホットメ
ルト型接着剤、溶剤型接着剤又は水性接着剤である。一
つの好ましい実施態様においては、剥離コーティング層
が存在し、これは、例えば、アンダーソンデベロップメ
ント(Anderson Development)のESCOAT P-2
0(商標)やマゾコーポレーション(Mazo Corporatio
n)のRA95-H(商標)等のポリビニールオクタデシ
ル剥離コーティングなどのカルバメート系剥離コーティ
ングから構成される。もう一つの好ましい実施態様にお
いては、テープ製品は剥離コーティングを持たない。Referring now to FIG. 2, the films of the present invention can be incorporated into a tape product 20, which exhibits the advantageous properties described above. The tape product depicted in this figure comprises a base layer 11, a reinforcing layer 12, an adhesive layer 21, a primer layer 22, and an optional adhesive repellent release coating layer 23. Adhesive layer, primer layer,
And for the optional release coating layer,
Any conventional materials may be used. This adhesive is
It is preferable to select from the group consisting of a natural rubber-based adhesive, a synthetic rubber-based adhesive and an acrylic adhesive, and a hot-melt adhesive, a solvent-based adhesive or a water-based adhesive. In one preferred embodiment, a release coating layer is present, such as, for example, ESCOAT P-2 from Anderson Development.
0 (trademark) or Mazo Corporation
n) consists of a carbamate-based release coating such as a polyvinyl octadecyl release coating such as RA95-H ™. In another preferred embodiment, the tape product has no release coating.
【0038】本発明テープ類は、例えば、引き裂きや補
強のためなどの種々の周知の目的のために、製造物品類
に適用される。図3に描かれる好ましい実施態様におい
ては、製造物品は、本発明テープ製品のストリップ31
によって互いに個々の袋32を連結した一連の包装袋3
0である。図4に描かれるもう一つの好ましい実施態様
においては、製造物品は密封後それを開封するための引
裂つまみ(tear tab)41を包含する封筒40であり、
引裂つまみ41は本発明によるテープ製品42によって
補強されている。これらと同様の引裂テープ類(tear t
apes)は良く知られており、例えば、封筒類だけでな
く、洗剤箱類、シガレットパッケージ類等の多くタイプ
のパッケージ類を開くのに用いられている。図5に描か
れるもう一つの好ましい実施態様においては、製造物品
は手提げ帯域(handle region)に開口51を有するシ
ョッピングバック50であり、その開口部は垂直方向テ
ープ製品ストリップ52と水平方向テープ製品ストリッ
プ53により全側辺部を補強されている。この種の補強
は、例えば、ショッピングバック類のみならず、写真ア
ルバム類の小口(edges)、ノートブック用紙の穴等の
あらゆるタイプの物品類に有用である。The tapes of the present invention are applied to articles of manufacture for various well-known purposes, such as, for example, for tearing and reinforcing. In the preferred embodiment depicted in FIG. 3, the article of manufacture is a strip 31 of the tape product of the present invention.
Series of packaging bags 3 in which individual bags 32 are connected to each other by
0. In another preferred embodiment depicted in FIG. 4, the article of manufacture is an envelope 40 containing a tear tab 41 for opening it after sealing.
The tear knob 41 is reinforced by a tape product 42 according to the present invention. Tear tapes similar to these
apes) are well known and are used to open many types of packages, such as detergent boxes, cigarette packages, as well as envelopes. In another preferred embodiment depicted in FIG. 5, the article of manufacture is a shopping bag 50 having an opening 51 in a handle region, the openings being a vertical tape product strip 52 and a horizontal tape product strip. 53 reinforces all sides. This type of reinforcement is useful, for example, in all types of articles, such as edges in photo albums, holes in notebook paper, as well as shopping bags.
【0039】共押出フィルムをテープ類に裁断する際
は、微細切り目の形成を避ける様な正規ブレード(regu
lar blade)を用いるのが好ましい。正規ブレードは微
細切り目の実質的に無い、歯直角エッジ(normal edg
e)を形成する。上記のことにも拘らず、意図的にテー
プ類を横方向に容易に引き裂くことができるように微細
切り目を形成するのが望ましい場合は、例えば、鋸歯状
ブレード(serrated blade)を用いてフィルムをテープ
類に裁断することできる。When cutting the coextruded film into tapes, use a regular blade (regu
Preferably, a lar blade is used. A regular blade has a normal edg with substantially no fine cuts.
e) forming. Notwithstanding the above, if it is desired to form a fine notch so that the tapes can be intentionally easily torn in the lateral direction, the film may be cut using, for example, a serrated blade. It can be cut into tapes.
【0040】次に、下記の限定的ではない実施例を参照
して更に詳細に本発明を説明する。 実施例 耐衝撃性変性ポリプロピレン〔シェル社の7C06(商
標)樹脂〕、リニア低密度ポリエチレン〔ダウ社の20
32(商標)樹脂〕及び着色剤〔スペクトラム社の10
51672 Red(商標)〕のブレンドから、153
0mm巾の基層を主押出機から押し出した。耐衝撃性変
性ポリプロピレン対リニア低密度ポリエチレンの比は、
重量%で93対7であった。この主押出機は5帯域から
なり、これらは215と250℃の間の温度で運転し
た。The invention will now be described in more detail with reference to the following non-limiting examples. Examples Impact modified polypropylene (Shell 7C06 ™ resin), linear low density polyethylene [Dow 20
32 (trademark) resin] and a colorant [10
51672 Red ™] from the blend
A 0 mm wide base layer was extruded from the main extruder. The ratio of impact modified polypropylene to linear low density polyethylene is
It was 93 to 7 by weight%. The main extruder consisted of five zones, which ran at temperatures between 215 and 250 ° C.
【0041】この基層上に、7C06(商標)樹脂、2
032(商標)樹脂及び脱フィブリル化剤(defibrilla
ting agent)〔これもまたシェル社のHY6100(商
標)樹脂〕のブレンドから1530mm巾の強化層を同
時押出機から同時押し出しした。7C06(商標):2
032(商標):HY6100(商標)の比は、重量パ
ーセントで39.6:60.3:0.1であった。この
同時押出機は3帯域からなり、これらも215と250
℃の間の温度で運転した。On this base layer, 7C06 ™ resin, 2C
032 ™ resin and defibrillating agent (defibrilla)
A 1530 mm wide reinforcement layer was co-extruded from a co-extruder from a blend of ting agent (also a HY6100 ™ resin from Shell). 7C06 ™: 2
The 032 ™: HY6100 ™ ratio was 39.6: 60.3: 0.1 by weight. This co-extruder consists of three zones, which are also 215 and 250
Operated at a temperature between ° C.
【0042】押し出し後、先ずフィルムを35〜40℃
に冷却し、それから80〜85℃で運転されている2本
の冷却ロールと1本の艶出ロール(glazing roll)を通
した。その後、フィルムを108℃前後で運転されてい
る予熱ロールに通し、それから120℃で延伸を施し
た。これに続いて、フィルムを130℃で運転されてい
るアニールロール上を通過させ、次いで一連の徐々に冷
たい冷却ロール上を通過させることによりアニールし
た。After extrusion, the film was first heated to 35 to 40 ° C.
And then passed through two chill rolls and one glazing roll operating at 80-85 ° C. Thereafter, the film was passed through a preheating roll operating at around 108 ° C and then stretched at 120 ° C. Following this, the film was annealed by passing it over an annealing roll operating at 130 ° C. and then passing over a series of gradually cold chill rolls.
【0043】押し出された材料の量を変化させ、それぞ
れの厚みが63、72及び120μmである3種の本発
明テープ類を製作した。比較のために、いずれも強化層
を持たない(”PE無し”)63μmと120μmのフ
ィルムも押し出した。63μmのPE無しフィルムは、
HY6100(商標)の80重量%と2032(商標)
の20重量%からなるものであった。120μmのPE
無しフィルムは、7C06(商標)と少量の着色剤から
なるものであった。得られたフィルム類は、表1に示す
特性を示した。By changing the amount of the extruded material, three kinds of tapes of the present invention having respective thicknesses of 63, 72 and 120 μm were produced. For comparison, 63 μm and 120 μm films without any reinforcement layer (“no PE”) were also extruded. 63 μm PE-free film is
80% by weight of HY6100 ™ and 2032 ™
Of 20% by weight. 120 μm PE
The neat film consisted of 7C06 ™ and a small amount of colorant. The resulting films exhibited the properties shown in Table 1.
【0044】[0044]
【表1】 1PEは、表示された厚みのポリエチレン層の存在を示
す。[Table 1] 1 PE indicates the presence of a polyethylene layer of the indicated thickness.
【0045】本明細書及び請求の範囲は説明として記載
されたもので、限定するものではなく、本発明の精神と
範囲から逸脱すること無く種々の改変や変更を行っても
よいことが認められるであろう。The specification and claims are provided by way of explanation, not limitation, and it is recognized that various modifications and changes may be made without departing from the spirit and scope of the invention. Will.
【図1】図1は、本発明による2層フィルムの概略図で
ある。FIG. 1 is a schematic diagram of a two-layer film according to the present invention.
【図2】図2は、本発明による5層テープ製品の概略図
である。FIG. 2 is a schematic diagram of a five-layer tape product according to the present invention.
【図3】図3は、本発明によるテープ製品の2本のスト
リップによって互いに連結された一連の3個の包装袋の
概略図である。FIG. 3 is a schematic view of a series of three packaging bags connected to each other by two strips of tape product according to the present invention.
【図4】図4は、密封され、それから本発明によるテー
プ製品で補強されたテープを引っ張ることにより開封す
る様に改造された封筒の概略図である。FIG. 4 is a schematic view of an envelope that has been sealed and then modified to be opened by pulling on a tape reinforced with a tape product according to the present invention.
【図5】図5は、本発明によるテープ製品のストリップ
で手提げ開口部(handle opening)の周りを補強したシ
ョッピングバッグの概略図である。FIG. 5 is a schematic view of a shopping bag reinforced around a handle opening with a strip of tape product according to the present invention.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 トランパー,リチャード,アラン,ジュニ ア アメリカ合衆国 49330 ミシガン州 ケ ントシティー,ウェーガルロード 12969 Fターム(参考) 4F100 AK03A AK03B AK04A AK04B AK07A AK07B AK25G AL01A AL01B AL05A AL05B AN01G AN02G AT00A BA03 BA07 BA10A BA10B BA10C BA25 CB01G CB03G CB10H EH20 EH202 GB15 JK02B JL14C YY00A YY00B 4J004 AA04 AA05 AA10 AB03 CC03 4J040 CA011 CA031 DF001 JA03 JA09 JB01 ──────────────────────────────────────────────────続 き Continuation of front page (72) Inventor Trumper, Richard, Allan, Jr. United States 49330 Wengal Road, Kent City, Michigan 12969 F-term (reference) 4F100 AK03A AK03B AK04A AK04B AK07A AK07B AK25G AL01A AL01B AL05A AL05B AN01G AN02G AT00A BA03 BA07 BA10A BA10B BA10C BA25 CB01G CB03G CB10H EH20 EH202 GB15 JK02B JL14C YY00A YY00B 4J004 AA04 AA05 AA10 AB03 CC03 4J040 CA011 CA031 DF001 JA03 JA09 JB01
Claims (21)
あって、(B)が(A)よりも強靭な材料から成り、
(B)が(A)の表面上に連続層を形成し、且つ、
(B)の厚みが(A)+(B)の合計厚みの25%より
小さいフィルム。1. A film comprising: (A) a base layer; and (B) a reinforcing layer adhered to (A), wherein (B) is made of a material that is stronger than (A),
(B) forms a continuous layer on the surface of (A), and
A film in which the thickness of (B) is less than 25% of the total thickness of (A) + (B).
ン共重合体を包含する請求項1によるフィルム。2. The film according to claim 1, wherein the base layer (A) comprises a polypropylene-olefin copolymer.
ンを更に含む請求項2によるフィルム。3. The film according to claim 2, wherein the base layer (A) further comprises a blended polyethylene.
エチレン対ポリプロピレン−オレフィン共重合体の比
が、25:75〜5:95の範囲にある請求項3による
フィルム。4. The film according to claim 3, wherein the ratio of the blended polyethylene to the polypropylene-olefin copolymer in the base layer (A) is in the range from 25:75 to 5:95.
請求項1によるフィルム。5. The film according to claim 1, wherein the reinforcing layer (B) comprises polyethylene.
ピレン−オレフィン共重合体を更に含む請求項5による
フィルム。6. The film according to claim 5, wherein the reinforcing layer (B) further comprises a blended polypropylene-olefin copolymer.
リプロピレン−オレフィン共重合体対ポリエチレンの比
が、50:50〜25:75の範囲にある請求項6によ
るフィルム。7. The film according to claim 6, wherein the ratio of blended polypropylene-olefin copolymer to polyethylene in the reinforcing layer (B) is in the range from 50:50 to 25:75.
25μmの範囲にあり、該補強層(B)の厚みが約2μ
m〜約10μmの範囲にある請求項1〜7のいずれか一
つによるフィルム。8. The base layer (A) has a thickness of about 60 μm to about 1 μm.
25 μm, and the thickness of the reinforcing layer (B) is about 2 μm.
A film according to any one of claims 1 to 7, ranging from m to about 10 [mu] m.
μmの範囲にある請求項8によるフィルム。9. The reinforcing layer (B) has a thickness of about 3 μm to about 5 μm.
9. A film according to claim 8 in the range of μm.
押し出しすることにより作製される請求項8によるフィ
ルム。10. The film according to claim 8, which is produced by co-extruding said base layer (A) with said reinforcing layer (B).
によるフィルム、および、 (B)フィルム(A)上にコーティングされた接着剤を
包含するテープ製品。11. A tape product comprising (A) a film according to any one of claims 1 to 10, and (B) an adhesive coated on the film (A).
ゴム系接着剤、および、アクリル系接着剤からなる群か
ら選ばれる請求項11によるテープ製品。12. The tape product according to claim 11, wherein said adhesive is selected from the group consisting of a natural rubber adhesive, a synthetic rubber adhesive, and an acrylic adhesive.
溶剤型接着剤、または、水性接着剤である請求項12に
よるテープ製品。13. The adhesive according to claim 13, wherein the adhesive is a hot melt adhesive.
13. The tape product according to claim 12, which is a solvent-based adhesive or a water-based adhesive.
るのと反対側のフィルム(A)上にコーティングされた
接着剤反発性剥離材料を更に包含する請求項11による
テープ製品。14. The tape product according to claim 11, further comprising an adhesive-repellent release material coated on the film (A) opposite to the side coated with the adhesive (B).
ト系剥離コーティングである請求項14によるテープ製
品。15. The tape product according to claim 14, wherein the adhesive-repellent release material is a carbamate-based release coating.
ゴム系接着剤、および、アクリル系接着剤からなる群か
ら選ばれる請求項15によるテープ製品。16. The tape product according to claim 15, wherein the adhesive is selected from the group consisting of a natural rubber adhesive, a synthetic rubber adhesive, and an acrylic adhesive.
溶剤型接着剤、または、水性接着剤である請求項16に
よるテープ製品。17. The adhesive according to claim 17, wherein the adhesive is a hot melt adhesive.
17. The tape product according to claim 16, which is a solvent-based adhesive or a water-based adhesive.
るテープ製品を包含する製造物品。18. Article of manufacture comprising a tape product according to any one of claims 11 to 17.
一連の包装袋を包含する請求項18による製造物品。19. The article of manufacture according to claim 18, comprising a series of packaging bags glued in series by said tape product.
プ製品の一端を引っ張ることにより開封される様に改造
されたシールパッケージを包含する請求項18による製
造物品。20. An article of manufacture according to claim 18 including the tape product and including a sealed package adapted to be opened by pulling one end of the tape product.
する請求項18による製造物品。21. The article of manufacture according to claim 18, comprising a container reinforced with said tape product.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4924197P | 1997-06-09 | 1997-06-09 | |
| US60/049,241 | 1997-06-09 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50277799A Division JP2001505500A (en) | 1997-06-09 | 1998-06-08 | Coextruded films, and tape products and manufactured articles containing them |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2002347180A true JP2002347180A (en) | 2002-12-04 |
Family
ID=21958788
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50277799A Pending JP2001505500A (en) | 1997-06-09 | 1998-06-08 | Coextruded films, and tape products and manufactured articles containing them |
| JP2002066392A Pending JP2002347180A (en) | 1997-06-09 | 2002-03-12 | Coextrusion film or the like, and tape products and manufactured goods or the like including them |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50277799A Pending JP2001505500A (en) | 1997-06-09 | 1998-06-08 | Coextruded films, and tape products and manufactured articles containing them |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP0988147B1 (en) |
| JP (2) | JP2001505500A (en) |
| CN (1) | CN1264334A (en) |
| AT (1) | ATE315476T1 (en) |
| AU (1) | AU744161B2 (en) |
| CA (1) | CA2293804A1 (en) |
| DE (1) | DE69833196T2 (en) |
| WO (1) | WO1998056581A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011511721A (en) * | 2008-01-22 | 2011-04-14 | テーザ・ソシエタス・ヨーロピア | Support film especially for adhesive tape and use thereof |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6354739B1 (en) | 1998-05-28 | 2002-03-12 | 3M Innovative Properties Company | Tear control closing tape and container with tear control closing tape |
| US6416857B1 (en) | 2000-10-25 | 2002-07-09 | 3M Innovative Properties Company | Tamper indicating device |
| US6513657B2 (en) | 2001-04-26 | 2003-02-04 | 3M Innovative Properties Co. | Product packaging with handle-forming tearable tape system |
| BRPI0409596A (en) | 2003-04-21 | 2006-05-02 | 3M Innovative Properties Co | violation indicating device, and article |
| DE102006061812A1 (en) * | 2006-12-21 | 2008-07-03 | Tesa Ag | Multi-layered adhesive tape |
| EP2551024B1 (en) | 2011-07-29 | 2017-03-22 | 3M Innovative Properties Co. | Multilayer film having at least one thin layer and continuous process for forming such a film |
| MX382817B (en) | 2012-07-06 | 2025-03-13 | Intertape Polymer Corp | CARTON SEALING TAPE. |
| EP2735595A1 (en) | 2012-11-23 | 2014-05-28 | 3M Innovative Properties Company | Multilayer pressure-sensitive adhesive assembly |
| CN105566744B (en) * | 2014-10-15 | 2018-03-02 | 中国石油化工股份有限公司 | A kind of polypropylene self-reinforced composite material and preparation method thereof |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4410582A (en) * | 1980-12-10 | 1983-10-18 | Toray Industries, Inc. | Multi-layered polyolefin laminated film |
| US4584220A (en) * | 1982-01-15 | 1986-04-22 | Kroy Inc. | Laminated tape |
| IT1181945B (en) * | 1984-12-31 | 1987-09-30 | Manuli Autoadesivi Spa | IMPROVEMENT IN SELF-ADHESIVE TAPES |
| DE3640861A1 (en) * | 1986-11-29 | 1988-06-09 | Beiersdorf Ag | Tear strips |
| US4828928A (en) * | 1986-12-17 | 1989-05-09 | W. R. Grace & Co. | Monoaxial shrink film |
-
1998
- 1998-06-08 AT AT98926203T patent/ATE315476T1/en not_active IP Right Cessation
- 1998-06-08 CN CN98807250A patent/CN1264334A/en active Pending
- 1998-06-08 WO PCT/US1998/011332 patent/WO1998056581A1/en not_active Ceased
- 1998-06-08 DE DE69833196T patent/DE69833196T2/en not_active Expired - Lifetime
- 1998-06-08 JP JP50277799A patent/JP2001505500A/en active Pending
- 1998-06-08 CA CA002293804A patent/CA2293804A1/en not_active Abandoned
- 1998-06-08 AU AU78097/98A patent/AU744161B2/en not_active Ceased
- 1998-06-08 EP EP98926203A patent/EP0988147B1/en not_active Expired - Lifetime
-
2002
- 2002-03-12 JP JP2002066392A patent/JP2002347180A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011511721A (en) * | 2008-01-22 | 2011-04-14 | テーザ・ソシエタス・ヨーロピア | Support film especially for adhesive tape and use thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1264334A (en) | 2000-08-23 |
| DE69833196T2 (en) | 2006-08-24 |
| EP0988147B1 (en) | 2006-01-11 |
| AU7809798A (en) | 1998-12-30 |
| CA2293804A1 (en) | 1998-12-17 |
| EP0988147A4 (en) | 2000-07-19 |
| WO1998056581A1 (en) | 1998-12-17 |
| JP2001505500A (en) | 2001-04-24 |
| EP0988147A1 (en) | 2000-03-29 |
| AU744161B2 (en) | 2002-02-14 |
| ATE315476T1 (en) | 2006-02-15 |
| DE69833196D1 (en) | 2006-04-06 |
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